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Klor Con M
Klor Con M - 0615-3599-39 - (potassium chloride)
Drug Information of Klor Con M
| Product NDC: | 0615-3599 |
| Proprietary Name: | Klor Con M |
| Non Proprietary Name: | potassium chloride |
| Active Ingredient(s): | 20 meq/1 & nbsp; potassium chloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Klor Con M
| Product NDC: | 0615-3599 |
| Labeler Name: | NCS HealthCare of KY, Inc dba Vangard Labs |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074726 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19981120 |
Package Information of Klor Con M
| Package NDC: | 0615-3599-39 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-3599-39) |
NDC Information of Klor Con M
| NDC Code | 0615-3599-39 |
| Proprietary Name | Klor Con M |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-3599-39) |
| Product NDC | 0615-3599 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | potassium chloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19981120 |
| Marketing Category Name | ANDA |
| Labeler Name | NCS HealthCare of KY, Inc dba Vangard Labs |
| Substance Name | POTASSIUM CHLORIDE |
| Strength Number | 20 |
| Strength Unit | meq/1 |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
